GB716505A - Improvements in or relating to hydroforming process - Google Patents

Improvements in or relating to hydroforming process

Info

Publication number
GB716505A
GB716505A GB25955/51A GB2595551A GB716505A GB 716505 A GB716505 A GB 716505A GB 25955/51 A GB25955/51 A GB 25955/51A GB 2595551 A GB2595551 A GB 2595551A GB 716505 A GB716505 A GB 716505A
Authority
GB
United Kingdom
Prior art keywords
catalyst
gas
zone
reactor
zones
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB25955/51A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB716505A publication Critical patent/GB716505A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G35/00Reforming naphtha
    • C10G35/04Catalytic reforming
    • C10G35/10Catalytic reforming with moving catalysts
    • C10G35/14Catalytic reforming with moving catalysts according to the "fluidised-bed" technique
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/90Regeneration or reactivation
    • B01J23/96Regeneration or reactivation of catalysts comprising metals, oxides or hydroxides of the noble metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/18Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
    • B01J8/1836Heating and cooling the reactor

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Combustion & Propulsion (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

<PICT:0716505/IV (b)/1> Naphtha is hydroformed in the presence of a dense fluidized catalyst which is withdrawn from the reaction zone, stripped of entrained gases by means of a stripping gas, and regenerated by passing in countercurrent to an oxygen-containing regeneration gas in a series of superimposed regeneration zones, in the complete absence of steam, the said gas entering the final and lowermost zone at a high temperature and passing through preceding zones at progressively lower temperatures to the first and uppermost zone maintained at 850-1000 DEG F. and the stripped catalyst entering the said first zone and passing to said final zone, being maintained in a fluidized state in said zones by the regeneration gas, and hydrogen completely removed in said first zone and residual carbon in succeeding zones, the regenerated catalyst then being recycled to the reaction zone. Naphtha is fed by pipe 14 and nozzles 15, and catalyst in suspension in hydrogen-rich gas by line 17 to reactor 10 to give a dense, fluidized bed 18. A ported conduit 23 serves to take off catalyst which is stripped by a countercurrent of steam or inert gas from pipe 26. The stripped catalyst passes by line 33 to regenerator 35 having perforated plates 36-39 with downcomers for conveying solids to the next lower plate. Oxygen-containing regeneration gas passes upwards from pipe 40 at a velocity to maintain a dense, fluidized catalyst bed on each plate. Combustion gases leave at the top and, if desired, may be used as stripping gas in conduit 23. The regeneration zones are operated at progressively higher temperatures, e.g. 850-1000 DEG F. in the top zone, and 1200 DEG F. in the bottom. Fresh feed may pass through coils 42-44 arranged in the catalyst beds whereby it is preheated while recycle gas is similarly heated in coils 47-49 before passing to line 17 where it effects a reconditioning of the catalyst while carrying it to reactor 10. In starting up, catalyst is fed through line 17 by an air stream, and hot air fed by line 40 until the reactor and regenerator are filled. Standpipe 51 is now opened, and the reactor purged with inert gas. Oil or fuel gas is fed to the regenerator to heat the catalyst; and fuel-gas supplied for conveying catalyst from standpipe 51 to the reactor until the latter reaches 850 DEG F. when naphtha feed begins. Reaction conditions are 850-975 DEG F., 50-1000 p.s.i.g., and 0.15-1.5 lb./lb. catalyst/hour. The catalyst to oil ratio may be 0.5-3. Specification 590,882, [Group III], is referred to.ALSO:Naphtha is hydroformed in the presence of a dense fluidized catalyst which is withdrawn from the reaction zone, stripped of entrained gases by means of a stripping gas, and regenerated by passing in countercurrent to an oxygen-containing regeneration gas in a series of superimposed regeneration zones, in the complete absence of steam, the said gas entering the final and lower-most zone at a high temperature and passing through preceding zones at progressively lower temperatures to the first and uppermost zone maintained at 850-1000 DEG F., and the stripped catalyst entering the said first zone and passing to said final zone, being maintained in a fluidized state in said zones by the regeneration gas, and hydrogen completely removed in said first zone and residual carbon in succeeding zones, the regenerated catalyst then being recycled to the reaction zone. Naphtha is fed by pipe 14 and nozzles 15, and catalyst in suspension in hydrogen-rich gas by line 17 to reactor 10 to give a dense fluidized bed 18. A ported conduit 23 serves to take off catalyst which is stripped by a countercurrent of steam or inert gas from pipe 26. The stripped catalyst passes by line 33 to regenerator 35 having perforated plates 36-39 <PICT:0716505/III/1> with downcomers for conveying solids to the next lower plate. Oxygen-containing regeneration gas passes upwards from pipe 40 at a velocity to maintain a dense fluidized catalyst bed on each plate. Combustion gases leave at the top and, if desired, may be used as stripping gas in conduit 23. The regeneration zones are operated at progressively higher temperatures, e.g. 850-1000 DEG F. in the top zone, and 1200 DEG F. in the bottom. Fresh feed may pass through coils 42-44 arranged in the catalyst beds whereby it is preheated while recycle gas is similarly heated in coils 47-49 before passing to line 17 where it effects the reconditioning of the catalyst while carrying it to reactor 10. In starting up, catalyst is fed through line 17 by an air stream and hot air fed by line 40 until the reactor and regenerator are filled. Standpipe 51 is now opened, and the reactor purged with inert gas. Oil or fuel gas is fed to the regenerator to heat the catalyst, and fuel gas supplied for conveying catalyst from standpipe 51 to the reactor until the latter reaches 850 DEG F. when naphtha feed begins. Reaction conditions are 850-975 DEG F., 50-1000 p.s.i.g., and .15-1.5 lbs./lb. catalyst/hr. The catalyst to oil ratio may be 0.5-3. Specification 590,882 is referred to.
GB25955/51A 1951-01-25 1951-11-06 Improvements in or relating to hydroforming process Expired GB716505A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US716505XA 1951-01-25 1951-01-25

Publications (1)

Publication Number Publication Date
GB716505A true GB716505A (en) 1954-10-06

Family

ID=22102693

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25955/51A Expired GB716505A (en) 1951-01-25 1951-11-06 Improvements in or relating to hydroforming process

Country Status (4)

Country Link
BE (1) BE507656A (en)
FR (1) FR1048954A (en)
GB (1) GB716505A (en)
NL (1) NL82686C (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1028726B (en) * 1955-08-26 1958-04-24 Exxon Research Engineering Co Process for the catalytic hydroforming of raw gasoline
BE594556A (en) * 1956-01-06

Also Published As

Publication number Publication date
NL82686C (en)
BE507656A (en)
FR1048954A (en) 1953-12-28

Similar Documents

Publication Publication Date Title
US4388218A (en) Regeneration of cracking catalyst in two successive zones
US2378342A (en) Catalytic conversion process and apparatus
US2902432A (en) Catalytic conversion of hydrocarbons
CN105585396B (en) A kind of method by oxygenatedchemicals preparing low-carbon olefins
US2397352A (en) Chemical process
US2432135A (en) Distillation of oil shale in fluidized condition with simultaneous combustion of spent shale
US3197284A (en) Fluidized catalytic hydrogen production
US3964876A (en) Method and apparatus for catalytically cracking hydrocarbons
GB2191214A (en) Production of higher molecular weight hydrocarbons from methane
US2730556A (en) Method for effecting endothermic dehydrogenation reactions
US1874801A (en) Process for the decomposition of hydrocarbons
US2434567A (en) Method and apparatus for contacting hydrocarbons with catalyst particles
US2526881A (en) Catalytic conversion of hydrocarbons to produce alkyl naphthalenes
US2788311A (en) Fluid system
US3129060A (en) Control of conversion in a catalytic hydrogen producing unit
US2537153A (en) Fluidized carbonization process
US2794709A (en) Preparation of carbon black and hydrogen
US2445351A (en) Process of adding heat in the regeneration of catalyst for the conversion of hydrocarbons
GB716505A (en) Improvements in or relating to hydroforming process
US2908617A (en) System for recovering oil from solid oil-bearing materials
US2697655A (en) Manufacture of a hydrogen-rich gas
US2873247A (en) Single vessel coking process
US2448553A (en) Process for recycling catalyst fines in a catalyst conversion system
US2456707A (en) Process for stripping spent fluid catalysts
US4975181A (en) Process and apparatus for ethylene production